Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome

Acta Neuropathol. 2020 Apr;139(4):795-797. doi: 10.1007/s00401-019-02118-5. Epub 2020 Jan 3.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Astrocytoma / complications
  • Astrocytoma / genetics*
  • Brain Neoplasms / complications
  • Brain Neoplasms / genetics*
  • Child
  • Female
  • Humans
  • Isocitrate Dehydrogenase / genetics*
  • Li-Fraumeni Syndrome / complications
  • Li-Fraumeni Syndrome / genetics*
  • Male
  • Mutation
  • Tumor Suppressor Protein p53 / genetics*

Substances

  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Isocitrate Dehydrogenase
  • IDH1 protein, human